Found: 12
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An automated 13.5 hour system for scalable diagnosis and acute management guidance for genetic diseases.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-31446-6
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- Article
An automated 13.5 hour system for scalable diagnosis and acute management guidance for genetic diseases.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-31446-6
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- Publication type:
- Article
The Limits of Economic Sanctions Under International Humanitarian Law: The Case of the Congo.
- Published in:
- Texas International Law Journal, 2012, v. 48, n. 1, p. 103
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- Article
Memory recovery in relation to default mode network impairment and neurite density during brain tumor treatment.
- Published in:
- Journal of Neurosurgery, 2022, v. 136, n. 2, p. 358, doi. 10.3171/2021.1.JNS203959
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- Article
Scalable, high quality, whole genome sequencing from archived, newborn, dried blood spots.
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- NPJ Genomic Medicine, 2023, v. 8, n. 1, p. 1, doi. 10.1038/s41525-023-00349-w
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- Article
Measurement of genetic diseases as a cause of mortality in infants receiving whole genome sequencing.
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- NPJ Genomic Medicine, 2020, v. 5, n. 1, p. N.PAG, doi. 10.1038/s41525-020-00155-8
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- Article
Reclassification of the Etiology of Infant Mortality With Whole-Genome Sequencing.
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- JAMA Network Open, 2023, v. 6, n. 2, p. e2254069, doi. 10.1001/jamanetworkopen.2022.54069
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- Article
Assessment of neuropsychological function in brain tumor treatment: a comparison of traditional neuropsychological assessment with app-based cognitive screening.
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- Acta Neurochirurgica, 2022, v. 164, n. 8, p. 2021, doi. 10.1007/s00701-022-05162-5
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- Article
Intraoperative mapping of executive function using electrocorticography for patients with low-grade gliomas.
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- Acta Neurochirurgica, 2021, v. 163, n. 5, p. 1299, doi. 10.1007/s00701-020-04646-6
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- Article
Abnormal Brain Structure and Function in Newborns With Complex Congenital Heart Defects Before Open Heart Surgery: A Review of the Evidence.
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- Journal of Child Neurology, 2011, v. 26, n. 6, p. 743, doi. 10.1177/0883073811402073
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- Article
Retrospective identification of prenatal fetal anomalies associated with diagnostic neonatal genomic sequencing results.
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 6, p. 705, doi. 10.1002/pd.6111
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- Article
Postmortem whole-genome sequencing on a dried blood spot identifies a novel homozygous SUOX variant causing isolated sulfite oxidase deficiency.
- Published in:
- Cold Spring Harbor Molecular Case Studies, 2021, v. 7, n. 3, p. 1, doi. 10.1101/mcs.a006091
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- Article